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苔藓纤维接触触发发育中小脑颗粒神经元中Kv4.2钾通道向树突和突触的靶向定位。

Mossy fibre contact triggers the targeting of Kv4.2 potassium channels to dendrites and synapses in developing cerebellar granule neurons.

作者信息

Shibasaki Koji, Nakahira Kensuke, Trimmer James S, Shibata Riichi, Akita Masumi, Watanabe Shu-Ichi, Ikenaka Kazuhiro

机构信息

Department of Physiological Sciences, the Graduate University for Advanced Studies, Okazaki, Japan.

出版信息

J Neurochem. 2004 May;89(4):897-907. doi: 10.1111/j.1471-4159.2004.02368.x.

Abstract

Compartmentalization of neuronal function is achieved by highly localized clustering of ion channels in discrete subcellular membrane domains. Voltage-gated potassium (Kv) channels exhibit highly variable cellular and subcellular patterns of expression. Here, we describe novel activity-dependent synaptic targeting of Kv4.2, a dendritic Kv channel, in cerebellar granule cells (GCs). In vivo, Kv4.2 channels are highly expressed in cerebellar glomeruli, specializations of GC dendrites that form synapses with mossy fibres. In contrast, in cultured GCs, Kv4.2 was found localized, not to dendrites but to cell bodies. To investigate the role of synaptic contacts, we developed a co-culture system with cells from pontine grey nucleus, the origin of mossy fibres. In these co-cultures, synaptic structures formed, and Kv4.2 was now targeted to these synaptic sites in a manner dependent on synaptic activity. Activation of NMDA- and/or AMPA-type glutamate receptors was necessary for the targeting of Kv4.2 in co-cultures, and activation of these receptor systems in GC monocultures induced dendritic targeting of Kv4.2 in the absence of synapse formation. These results indicate that the proper targeting of Kv4.2 channels is dynamically regulated by synaptic activity. This activity-dependent regulation of Kv4.2 localization provides a crucial yet dynamic link between synaptic activity and dendritic excitability.

摘要

神经元功能的区室化是通过离子通道在离散的亚细胞膜结构域中的高度局部聚集来实现的。电压门控钾(Kv)通道表现出高度可变的细胞和亚细胞表达模式。在这里,我们描述了小脑颗粒细胞(GCs)中树突状Kv通道Kv4.2的一种新的活性依赖性突触靶向。在体内,Kv4.2通道在小脑小球中高度表达,小脑小球是GC树突的特化结构,与苔藓纤维形成突触。相比之下,在培养的GCs中,发现Kv4.2不是定位于树突,而是定位于细胞体。为了研究突触接触的作用,我们开发了一种与来自苔藓纤维起源的脑桥灰质核的细胞共培养的系统。在这些共培养物中形成了突触结构,并且Kv4.2现在以依赖于突触活性的方式靶向这些突触位点。NMDA和/或AMPA型谷氨酸受体的激活对于共培养物中Kv4.2的靶向是必需的,并且在GC单培养物中这些受体系统的激活在没有突触形成的情况下诱导了Kv4.2的树突靶向。这些结果表明,Kv4.2通道的正确靶向是由突触活性动态调节的。Kv4.2定位的这种活性依赖性调节在突触活性和树突兴奋性之间提供了一个关键而动态的联系。

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